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Revision as of 15:07, 2 April 2024 by Maxim Masiutin(talk | contribs)(Added the cs1 style template to denote Vancouver ("vanc") citation style, because references contain "vauthors" attribute to specify the list of authors. Added bibcode. | Use this tool. Report bugs. | #UCB_Gadget)
This isoform of 17β-HSD is expressed predominantly in the testis and catalyzes the conversion of androstenedione to testosterone. It preferentially uses NADP as cofactor. Deficiency can result in impaired virilization of genetically male infants, formerly termed male pseudohermaphroditism.[8][7]
Ademola Akesode F, Meyer WJ, Migeon CJ (December 1977). "Male pseudohermaphroditism with gynaecomastia due to testicular 17-ketosteroid reductase deficiency". Clinical Endocrinology. 7 (6): 443–52. doi:10.1111/j.1365-2265.1977.tb01336.x. PMID598011. S2CID72297230.
Eckstein B, Cohen S, Farkas A, Rösler A (February 1989). "The nature of the defect in familial male pseudohermaphroditism in Arabs of Gaza". The Journal of Clinical Endocrinology and Metabolism. 68 (2): 477–85. doi:10.1210/jcem-68-2-477. PMID2918056.
Rösler A, Kohn G (July 1983). "Male pseudohermaphroditism due to 17 beta-hydroxysteroid dehydrogenase deficiency: studies on the natural history of the defect and effect of androgens on gender role". Journal of Steroid Biochemistry. 19 (1B): 663–74. doi:10.1016/0022-4731(83)90233-9. PMID6310248.
Bilbao JR, Loridan L, Audí L, Gonzalo E, Castaño L (September 1998). "A novel missense (R80W) mutation in 17-beta-hydroxysteroid dehydrogenase type 3 gene associated with male pseudohermaphroditism". European Journal of Endocrinology. 139 (3): 330–3. doi:10.1530/eje.0.1390330. PMID9758445. S2CID26522874.